US11530965B2 - Monitoring device for a system for generating medical compressed air - Google Patents
Monitoring device for a system for generating medical compressed air Download PDFInfo
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- US11530965B2 US11530965B2 US16/616,038 US201816616038A US11530965B2 US 11530965 B2 US11530965 B2 US 11530965B2 US 201816616038 A US201816616038 A US 201816616038A US 11530965 B2 US11530965 B2 US 11530965B2
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- 238000012806 monitoring device Methods 0.000 title claims abstract description 53
- 238000004378 air conditioning Methods 0.000 claims abstract description 13
- 238000011144 upstream manufacturing Methods 0.000 claims abstract description 6
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 claims description 25
- 229910002091 carbon monoxide Inorganic materials 0.000 claims description 25
- 238000012544 monitoring process Methods 0.000 claims description 13
- 230000006378 damage Effects 0.000 claims description 6
- 230000005540 biological transmission Effects 0.000 claims description 5
- 239000003570 air Substances 0.000 description 172
- 239000007789 gas Substances 0.000 description 15
- 230000008878 coupling Effects 0.000 description 10
- 238000010168 coupling process Methods 0.000 description 10
- 238000005859 coupling reaction Methods 0.000 description 10
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 6
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 4
- MWUXSHHQAYIFBG-UHFFFAOYSA-N Nitric oxide Chemical compound O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 239000012528 membrane Substances 0.000 description 3
- MGWGWNFMUOTEHG-UHFFFAOYSA-N 4-(3,5-dimethylphenyl)-1,3-thiazol-2-amine Chemical compound CC1=CC(C)=CC(C=2N=C(N)SC=2)=C1 MGWGWNFMUOTEHG-UHFFFAOYSA-N 0.000 description 2
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 2
- 239000012080 ambient air Substances 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 229910002092 carbon dioxide Inorganic materials 0.000 description 2
- 239000001569 carbon dioxide Substances 0.000 description 2
- JCXJVPUVTGWSNB-UHFFFAOYSA-N nitrogen dioxide Inorganic materials O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 description 2
- 239000012266 salt solution Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 229920000557 Nafion® Polymers 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000003780 insertion Methods 0.000 description 1
- 230000037431 insertion Effects 0.000 description 1
- 229910001629 magnesium chloride Inorganic materials 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 230000008054 signal transmission Effects 0.000 description 1
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N1/00—Sampling; Preparing specimens for investigation
- G01N1/02—Devices for withdrawing samples
- G01N1/22—Devices for withdrawing samples in the gaseous state
- G01N1/2247—Sampling from a flowing stream of gas
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M16/00—Devices for influencing the respiratory system of patients by gas treatment, e.g. ventilators; Tracheal tubes
- A61M16/0051—Devices for influencing the respiratory system of patients by gas treatment, e.g. ventilators; Tracheal tubes with alarm devices
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M16/00—Devices for influencing the respiratory system of patients by gas treatment, e.g. ventilators; Tracheal tubes
- A61M16/0057—Pumps therefor
- A61M16/0063—Compressors
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M16/00—Devices for influencing the respiratory system of patients by gas treatment, e.g. ventilators; Tracheal tubes
- A61M16/10—Preparation of respiratory gases or vapours
- A61M16/14—Preparation of respiratory gases or vapours by mixing different fluids, one of them being in a liquid phase
- A61M16/16—Devices to humidify the respiration air
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/0004—Gaseous mixtures, e.g. polluted air
- G01N33/0009—General constructional details of gas analysers, e.g. portable test equipment
- G01N33/0011—Sample conditioning
- G01N33/0018—Sample conditioning by diluting a gas
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/0004—Gaseous mixtures, e.g. polluted air
- G01N33/0009—General constructional details of gas analysers, e.g. portable test equipment
- G01N33/0027—General constructional details of gas analysers, e.g. portable test equipment concerning the detector
- G01N33/0036—General constructional details of gas analysers, e.g. portable test equipment concerning the detector specially adapted to detect a particular component
- G01N33/004—CO or CO2
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/0004—Gaseous mixtures, e.g. polluted air
- G01N33/0009—General constructional details of gas analysers, e.g. portable test equipment
- G01N33/0062—General constructional details of gas analysers, e.g. portable test equipment concerning the measuring method or the display, e.g. intermittent measurement or digital display
- G01N33/0063—General constructional details of gas analysers, e.g. portable test equipment concerning the measuring method or the display, e.g. intermittent measurement or digital display using a threshold to release an alarm or displaying means
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M16/00—Devices for influencing the respiratory system of patients by gas treatment, e.g. ventilators; Tracheal tubes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M16/00—Devices for influencing the respiratory system of patients by gas treatment, e.g. ventilators; Tracheal tubes
- A61M16/0003—Accessories therefor, e.g. sensors, vibrators, negative pressure
- A61M2016/003—Accessories therefor, e.g. sensors, vibrators, negative pressure with a flowmeter
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M2205/00—General characteristics of the apparatus
- A61M2205/33—Controlling, regulating or measuring
- A61M2205/3327—Measuring
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M2205/00—General characteristics of the apparatus
- A61M2205/84—General characteristics of the apparatus for treating several patients simultaneously
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/0004—Gaseous mixtures, e.g. polluted air
- G01N33/0009—General constructional details of gas analysers, e.g. portable test equipment
Definitions
- the present invention pertains to a device for monitoring a system for generating medical compressed air.
- the compressed air is removed from the compressed air system downstream of a compressed air conditioning unit and is fed to the monitoring device via a measured air line.
- the monitoring device has at least one sensor, which generates a measured signal as a function of a property of the compressed air being fed through the measured air line. This measured signal is analyzed and information about the compressed air is made available to a user by means of an output unit.
- Compressed air generating systems are used in hospitals to supply medical compressed air through a network of compressed air supply lines to different compressed air consumers within the hospital.
- the medical compressed air generated by the compressed air generating system is checked by a compressed air monitoring device for different parameters, and in particular for the concentration of relevant gases.
- Foreign gas concentrations of sulfur dioxide and nitrogen dioxide, for example, are detected in this manner to ensure that a medically flawless medical compressed air can be made available to the compressed air consumers.
- devices are used in the compressed air monitoring device to detect the relevant parameters of the medical compressed air.
- medical compressed air as a drug, is subject to the European Pharmacopoeia, so that correspondingly high requirements, which are listed in DIN EN ISO 7396-1, are placed on the quality of this compressed air.
- predefined concentrations of carbon dioxide, carbon monoxide, oil, sulfur dioxide, nitrogen oxide may not be exceeded.
- oxygen must be present in the compressed air with a content of 20.4 vol. % to 21.4 vol. %.
- this medical compressed air is purified by means of a treatment device with filters and dehumidified by a dehumidifier, wherein the moisture content is less than 67 ppm.
- a compressed air monitoring device which permanently monitors the compressed air generated by means of a compressed air conditioning system with regard to its properties and taking into account the legal regulations, is known from DE 10 2010 014 222 A1.
- the compressed air monitoring device being described has as an essential component a humidifier that humidifies the compressed air fed to the sensors via a measuring line, so that drying out of the sensors is avoided in a reliable manner.
- the humidifier in this case preferably has a semipermeable, water-impermeable membrane which absorbs no harmful gases, for example, carbon monoxide, sulfur dioxide or nitrogen dioxide, and, moreover, also does not let any harmful gases diffuse through to the other side in case of an excess pressure on one side of the membrane.
- a basic object of the present invention is to perfect a device for monitoring a system for supplying consumers with medical compressed air in that monitoring of the generated medical compressed air within legal regulations is made possible with relatively low technical effort and thus in a relatively cost-effective manner.
- taking compressed air samples shall be possible in a simple manner.
- a compact arrangement of the sensors and components shall be accomplished, and an advantageous technical solution shall be provided for monitoring the concentration of carbon monoxide in the compressed air.
- the present invention pertains to a compressed air monitoring device for a system for generating medical compressed air with a measured air line for removing compressed air from a compressed air supply line downstream of a compressed air conditioning unit.
- the compressed air monitoring device has at least one sensor for generating a measured signal as a function of a property of the compressed air fed through the measured air line, at least one humidifier for humidifying the compressed air upstream of the sensor and at least one output unit which outputs information about the property of the compressed air to a user on the basis of the measured signal.
- the present invention is characterized in that a tap is provided for removing compressed air and an actuator is provided for setting a volume flow and/or mass flow prevailing in the measured air line, wherein the actuator is inserted into the tap in a measuring mode and is removed from the tap in a compressed air removal mode.
- the essential technical feature of the present invention is thus based on the fact that a conventional tap, as it is also used for connection to compressed air consumers, is used for taking a compressed air sample, on the one hand, and an actuator (flowmeter) is inserted into the tap or into the compressed air port, on the other hand.
- the actuator is preferably configured such that different discrete desired values can be set for the volume flow and/or mass flow prevailing in the measured air line.
- the actuator is preferably configured such that volume flow values of 0 L/min, 0.1 L/min, 0.2 L/min, 0.3 L/min, 0.4 L/min, 0.5 L/min, 0.6 L/min, 0.8 L/min or 1 L/min can be set in the measured air line.
- a configuration of the actuator, in which at least desired values are set for the volume flow of 0.1 L/min or 0.2 L/min, is especially advantageous.
- the actuator has at least one diaphragm, which brings about an adjustment of the volume flow.
- the actuator may be manual, for example, by providing a switch, which can be locked or actuated in an automated manner in different positions. It is generally conceivable that the actuator can be actuated by an external apparatus via a suitable interface and that data can be exchanged, as needed, unidirectionally or bidirectionally between the actuator and an external apparatus. It is otherwise advantageous if the actuator has a display unit, via which at least one operating parameter, especially the set desired value of the volume flow and/or mass flow prevailing in the measured air line, is outputted at least at times. As needed, the actuator has in a suitable manner its own supply unit with battery or storage battery for supplying with electrical energy or is to be supplied with electrical energy via an external power supply.
- the tap is arranged downstream of the compressed air conditioning unit and upstream of the humidifier, which humidifies the compressed air before it is fed to the sensors. It is ensured in this manner that a compressed air sample can be taken, which has the parameters likewise present in the compressed air supply system.
- the actuator can advantageously be inserted into the tap and removed from the tap in a manner free from destruction and without using tools for setting the volume flow and/or mass flow prevailing in the measured air line.
- the corresponding actuator is inserted in a relatively simple manner into the tap, which is preferably configured as a conventional compressed air coupling, and can also be removed again.
- the at least one sensor is configured as an electrochemical sensor to detect a property of the compressed air.
- a sensor is characterized in that it generates a measuring current as a function of the gas concentration of a specific gas in the measured compressed air, which measuring current is present as a measured signal and is analyzed with a suitable analyzer.
- the measured signal thus obtained is finally fed to an output unit, which outputs information about the measured property of the compressed air, especially the concentration of the specific gas, to a user.
- At least one sensor is especially advantageously provided, which detects the concentration of carbon monoxide (CO) within the medical compressed air generated. It is essential here that the CO concentration within the air be provided downstream of all compressed air conditioning units.
- CO carbon monoxide
- a flowmeter is further provided, with which the volume flow and/or mass flow in the measuring gas line is measured and monitored. It is generally conceivable in this connection that the value measured by the flowmeter is used to monitor the setting of the actuator and to set to the needed value, as needed. Provisions are made in a very special embodiment of the presents invention for the value of the current volume flow, which value is determined by the flowmeter, to be used to adjust the actuator preferably in an automated manner, as least provided that the current value of the volume flow deviates from the desired value.
- the compressed air monitoring device has a sensor for detecting the CO concentration in the compressed air, a humidifier for humidifying the air in the measured gas line and a tap with an actuator, which can be inserted into the tap or can be removed from same.
- the above-mentioned components are preferably accommodated in a housing, so that a relatively compact unit is provided for monitoring the CO content of a compressed air flow, which at the same time makes it possible to be able to take a compressed air sample in a simple manner.
- a flowmeter is also preferably arranged in the housing to measure the volume flow of the compressed air within the measured air line.
- the compressed air monitoring device configured according to the present invention advantageously has at least one dew point sensor.
- the humidity of the compressed air is monitored in this manner, and it is ensured that the above-described moisture content is not exceeded. It is, in principle, also conceivable in this connection to measure the humidity of the compressed air in the measured gas line in the flow direction behind the humidifier and/or behind the sensor for detecting a property of the compressed air in order to ensure that the respectively necessary humidity is present, but it is not too high.
- the output unit is configured to display at least one concentration of a gas contained in the compressed air on a display unit or on a display. It is otherwise advantageous if the output unit is further configured to generate an alarm signal when exceeding or falling below a limit value for a property of the compressed air, especially the concentration of a specific gas.
- a transmission unit is, furthermore, provided, so that a corresponding alarm can be transmitted to an external apparatus. Such a transmission can be carried out both in a wired manner and in a wireless manner. It is absolutely conceivable here that such an alarm is transmitted to a central monitoring device, for example, with an alarm server, or to locally arranged apparatuses that are carried along by the monitoring staff in charge.
- the at least one sensor for detecting a property, especially a gas concentration, of the compressed air, the humidifier and the tap to be arranged in a housing.
- a housing is preferably a cabinet, especially a metal cabinet, which can be securely closed by means of a door.
- the necessary electronic components for controlling and for monitoring the compressed air monitoring device are likewise provided in such a housing. It is also conceivable that these components are arranged adjacent to the housing, in which the sensor for detecting a property of the compressed air, the humidifier and the tap are provided.
- infrared sensors As an alternative or in addition to using electrochemical sensors for detecting a property of the compressed air, it is likewise possible to use infrared sensors, which are thus based on an optical measuring principle.
- the present invention is generally not limited to the use of a special type of sensor. Rather, sensors, which use different measuring principles, can each be used for use in the compressed air monitoring device according to the present invention, provided that they can detect a property of the compressed air, especially the concentration of a gas present in the compressed air, in a suitable manner.
- the present invention also pertains to a compressed air generation system, which is combined with a compressed air monitoring device configured according to the present invention.
- a compressed air generation system for a hospital comprises here an air compressor, which is configured, for example, as a reciprocating compressor or as a screw-type compressor for compressing ambient air to form medical compressed air, a dehumidifier for dehumidifying the ambient air taken in and the compressed air monitoring device configured according to the present invention for monitoring at least one parameter of the medical compressed air.
- All alarms generated by the compressed air monitoring device are preferably transmitted to an alarm management system, which makes possible both a central and a local alarm generation.
- the recorded measured parameters and/or the respectively generated alarms are preferably documented continually, so that not only is a provision of medical compressed air ensured at any time, but also, moreover, aberrations within the compressed air generation system or compressed air provision system are detected at an early stage.
- FIG. 1 is a side view showing a compressed air monitoring device with integrated tap, into which an actuator for setting the volume flow is inserted;
- FIG. 2 is a side view showing a compressed air monitoring device with integrated tap, into which no actuator for setting the volume flow is inserted.
- FIG. 1 shows a compressed air monitoring device 1 configured according to the present invention, with which medical compressed air provided by a compressed air conditioning unit is monitored.
- the compressed air monitoring device 1 has for this purpose a sensor 2 for detecting a property of the compressed air, which is configured as an electrochemical sensor 2 according to this exemplary embodiment.
- the electrochemical sensor 2 can determine the concentration of carbon monoxide (CO) in the compressed air generated by the compressed air conditioning unit.
- the compressed air monitoring device 1 being shown is arranged downstream of the compressed air conditioning unit, which has essentially a compressor and a dehumidifier. No other technical devices are arranged between the compressed air conditioning unit and the compressed air monitoring device 1 shown in FIG. 1 .
- the compressed air monitoring device 1 essentially has a measured air line 3 , via which compressed air is removed from the compressed air supply system and is finally fed to the electrochemical sensor 2 for detecting the carbon monoxide concentration in the compressed air.
- the medical compressed air admitted into the compressed air supply lines from the compressed air generation system is reduced via a pressure reducer to a pressure of, for example, 1.2 bar with a volume flow of no more than about 1.0 L/min and is fed into the measured air line 3 .
- the volume flow within the measured air line 3 is first set to a value of 0.1 L/min or 0.2 L/min by means of the actuator 5 inserted into a tap 4 , which is configured as a compressed air coupling 14 .
- the volume flow prevailing in the measured air line is monitored by means of the flowmeter 6 . Provided that the setting of the volume flow is carried out in an automated manner, this takes place taking into account a desired volume flow value stored in the control unit 7 as well as the actual value of the volume flow, which actual value of the volume flow is measured by the flowmeter 6 .
- the CO sensor 2 with which the concentration of carbon dioxide in the compressed air is detected, is an essential component of the compressed air monitoring device 1 .
- a humidifier 8 is arranged upstream of the CO sensor 2 , with respect to the flow direction.
- the humidifier 8 has a fluidtight housing.
- the flexible tube also forms the measured air line 3 within the housing of the humidifier 8 .
- the medical compressed air is fed through the flexible tube through a space enclosed by the housing of the humidifier 8 .
- a saturated water-salt solution is located within the space enclosed by the housing of the humidifier 8 , wherein the salt, preferably magnesium chloride, is located on a bottom of the space enclosed by the housing of the humidifier 8 .
- Moist air with a constant relative humidity in the range of approximately 30% is located above the water-salt solution.
- medical compressed air with a volume flow of 0.1 L/min or 0.2 L/min is fed through the measured air line 3 and thus through the flexible tube in the interior of the humidifier 8 .
- the flexible tube is dimensioned such that it has a sufficient length and surface, so that the moisture of the moist air is diffused through the flexible tube into the medical compressed air and this compressed air is moistened to a relative humidity in the range between 25% and 30%.
- this moistened medical compressed air is forwarded via the measured air line 3 and at first is guided through the flowmeter 6 before it is sent to the CO sensor 2 .
- the sensor receives medical compressed air with a constant relative humidity in the range between 25% and 30%, so that the CO sensor 2 cannot dry out and can be used reliably over a longer time, which is preferably longer than six months. A frequent replacement of the CO sensor 2 can thus be reliably avoided.
- the actuator 5 is provided for setting the volume flow to be able to set the volume flow within the measured gas line 3 to a desired value.
- This actuator 5 has a port, which is configured such that the actuator 5 can be inserted into a conventional compressed air coupling 14 for compressed air consumers.
- a tool is neither necessary for an insertion of the actuator 5 into the conventional compressed air coupling 14 nor is a tool necessary for a removal of the actuator 5 out the conventional compressed air coupling 14 of the tap 4 .
- the actuator 5 is located in the inserted position in the tap 4 , which is configured as a compressed air coupling 14 .
- a constant volume flow is set within the measured air line 3 by the actuator 5 .
- Different discrete volume flow values of 0.1 L/min, 0.2 L/min, 0.3 L/min, 0.4 L/min, 0.5 L/min, 0.6 L/min, 0.8 L/min, or 1.0 L/min can be set with the actuator 5 , which has a diaphragm (diaphragm valve).
- a volume flow of 0.1 L/min or 0.2 L/min is preferably set at the actuator 5 .
- the respectively set desired value for the volume flow is monitored by means of the flowmeter 6 .
- a manual or automated adjustment of the actuator 5 can advantageously be carried out based on the values for the current volume flow, which values are determined with the flowmeter 6 . Furthermore, corresponding measured values may be transmitted to a central analyzer 9 by wire (in a wired manner or preferably wirelessly (in a wireless manner). Moreover, the measured signals generated by a suitably configured flowmeter 6 can be used to set the volume flow flowing through the measured air line 3 to the CO sensor 2 by means of the actuator 5 . The actuator 5 can be automatically adjusted (in an automated manner) with the measured signals generated by the flowmeter 6 based on the actuator having the diaphragm valve or another control valve.
- the compressed air monitoring device 1 shown in FIG. 1 for the permanent monitoring of the CO content of medical compressed air is arranged in a compact manner within a housing 10 .
- the CO sensor 2 , the tap 4 with the actuator 5 inserted in it, the humidifier 8 and the flowmeter 6 are thus arranged in the housing 10 , which can be closed by a door 13 .
- an illuminating unit 11 is provided in order to carry out work even under poor light conditions at the compressed air monitoring device 1 , especially to read measured values for the CO concentration from an output unit 12 or to take a compressed air sample via the tap 4 .
- the volume flow within the measured air line can advantageously be set by means of this actuator 5 . If the flowmeter 6 is coupled to the actuator 5 in a controlled manner, the volume flow in the measured air line 3 can be changed as a function of the measured signal generated by the flowmeter 6 .
- the degree of automation of the compressed air monitoring device 1 and also the manner of data transmission can generally be adapted to the conditions in the respective hospital.
- the CO sensor 2 may have different data interfaces as a function of these conditions or the present requirements.
- an analog measured signal of 4-20 mA can be generated or the signal transmission takes place via a BUS system, for example, HART, LON, Profibus or Foundation-Fieldbus.
- FIG. 2 shows a compressed air monitoring device 1 configured according to the present invention, which has the same components as they were already explained in connection with FIG. 1 .
- Identical components are identified by the same reference numbers. It is essential that just as in FIG. 1 , all components are arranged compactly in a closable housing 10 .
- the actuator 5 in the view according to FIG. 2 is not located within the tap 4 , which is configured as a compressed air coupling 14 . Rather, the compressed air coupling 14 is freely accessible in this operating state in the compressed air removal mode and can be used as a tap 4 for taking a compressed air sample from the compressed air system.
- the actuator 5 can in turn be inserted into the compressed air coupling, so that a constant volume flow again permanently flows through the measured air line 3 corresponding to the setting of the actuator 5 .
- the technical solution according to the present invention thus makes it possible to combine the measurement of a carbon monoxide concentration in medical compressed air with the possibility of taking individual compressed air samples in a relatively simple manner.
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Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102017005011.2A DE102017005011B3 (de) | 2017-05-24 | 2017-05-24 | Überwachungseinrichtung für eine Anlage zur Erzeugung medizinischer Druckluft |
| DE102017005011.2 | 2017-05-24 | ||
| PCT/EP2018/063438 WO2018215505A1 (de) | 2017-05-24 | 2018-05-23 | Überwachungseinrichtung für eine anlage zur erzeugung medizinischer druckluft |
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| US20200088611A1 US20200088611A1 (en) | 2020-03-19 |
| US11530965B2 true US11530965B2 (en) | 2022-12-20 |
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| US (1) | US11530965B2 (de) |
| EP (1) | EP3631441B1 (de) |
| CN (1) | CN110720037B (de) |
| DE (1) | DE102017005011B3 (de) |
| WO (1) | WO2018215505A1 (de) |
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| DE102019005014A1 (de) | 2019-07-19 | 2021-01-21 | Drägerwerk AG & Co. KGaA | Versorgungssystem, Betätigungseinheit und Verfahren zum Betreiben eines Versorgungssystems |
| US11760169B2 (en) | 2020-08-20 | 2023-09-19 | Denso International America, Inc. | Particulate control systems and methods for olfaction sensors |
| US12251991B2 (en) | 2020-08-20 | 2025-03-18 | Denso International America, Inc. | Humidity control for olfaction sensors |
| US12017506B2 (en) | 2020-08-20 | 2024-06-25 | Denso International America, Inc. | Passenger cabin air control systems and methods |
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| US12377711B2 (en) | 2020-08-20 | 2025-08-05 | Denso International America, Inc. | Vehicle feature control systems and methods based on smoking |
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| US11813926B2 (en) | 2020-08-20 | 2023-11-14 | Denso International America, Inc. | Binding agent and olfaction sensor |
| US11760170B2 (en) | 2020-08-20 | 2023-09-19 | Denso International America, Inc. | Olfaction sensor preservation systems and methods |
| US11828210B2 (en) | 2020-08-20 | 2023-11-28 | Denso International America, Inc. | Diagnostic systems and methods of vehicles using olfaction |
| US11932080B2 (en) | 2020-08-20 | 2024-03-19 | Denso International America, Inc. | Diagnostic and recirculation control systems and methods |
| CN112169104A (zh) * | 2020-09-28 | 2021-01-05 | 南通市第一人民医院 | 一种基于5g的重症病人呼吸暂停抢救装置及其使用方法 |
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Also Published As
| Publication number | Publication date |
|---|---|
| EP3631441A1 (de) | 2020-04-08 |
| DE102017005011B3 (de) | 2018-09-20 |
| CN110720037A (zh) | 2020-01-21 |
| WO2018215505A1 (de) | 2018-11-29 |
| CN110720037B (zh) | 2022-04-19 |
| US20200088611A1 (en) | 2020-03-19 |
| EP3631441B1 (de) | 2022-07-27 |
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